BR0208891A - Dihydro-benzo [b] - [1,4] diazepin-2-one derivatives as mglur2 ii antagonists - Google Patents
Dihydro-benzo [b] - [1,4] diazepin-2-one derivatives as mglur2 ii antagonistsInfo
- Publication number
- BR0208891A BR0208891A BR0208891-6A BR0208891A BR0208891A BR 0208891 A BR0208891 A BR 0208891A BR 0208891 A BR0208891 A BR 0208891A BR 0208891 A BR0208891 A BR 0208891A
- Authority
- BR
- Brazil
- Prior art keywords
- diazepin
- benzo
- derivatives
- antagonists
- dihydro
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
- C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
- C07D243/24—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Abstract
"DERIVADOS DE DIHIDRO-BENZO[B]-[1,4]DIAZEPIN-2-ONA COMO ANTAGONISTAS DE mGIuR2 II". Esta invenção refere-se a derivados de dihidro-benzo[b][1,4]diazepin-2-ona de fórmula geral, em que R1, R2, R3, X e Y são como definidos no relatório descritivo. A invenção também refere-se aos medicamentos contendo estes compostos, um processo para sua fabricação bem como seu uso para a preparação de medicamentos para o tratamento ou prevenção de distúrbios neurológicos agudos e/ou crónicos."DIHIDRO-BENZO DERIVATIVES [B] - [1,4] DIAZEPIN-2-ONA AS MGIuR2 II ANTAGONISTS". This invention relates to dihydro-benzo [b] [1,4] diazepin-2-one derivatives of general formula wherein R 1, R 2, R 3, X and Y are as defined in the specification. The invention also relates to medicaments containing these compounds, a process for their manufacture as well as their use for the preparation of medicaments for the treatment or prevention of acute and / or chronic neurological disorders.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01109125 | 2001-04-12 | ||
PCT/EP2002/003644 WO2002083652A1 (en) | 2001-04-12 | 2002-04-02 | DIHYDRO-BENZO [b] [1, 4] DIAZEPIN-2-ONE DERIVATIVES AS MGLUR2 ANTAGONISTS II |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0208891A true BR0208891A (en) | 2004-04-20 |
Family
ID=8177126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0208891-6A BR0208891A (en) | 2001-04-12 | 2002-04-02 | Dihydro-benzo [b] - [1,4] diazepin-2-one derivatives as mglur2 ii antagonists |
Country Status (38)
Country | Link |
---|---|
US (1) | US6544985B2 (en) |
EP (1) | EP1379511B1 (en) |
JP (1) | JP4071115B2 (en) |
KR (1) | KR100566171B1 (en) |
CN (1) | CN1264825C (en) |
AR (1) | AR035816A1 (en) |
AT (1) | ATE299868T1 (en) |
AU (1) | AU2002312788B2 (en) |
BG (1) | BG108254A (en) |
BR (1) | BR0208891A (en) |
CA (1) | CA2442557C (en) |
CZ (1) | CZ20033003A3 (en) |
DE (1) | DE60205100T2 (en) |
DK (1) | DK1379511T3 (en) |
EC (1) | ECSP034797A (en) |
ES (1) | ES2246012T3 (en) |
GT (1) | GT200200073A (en) |
HK (1) | HK1068888A1 (en) |
HR (1) | HRP20030792A2 (en) |
HU (1) | HUP0400851A3 (en) |
IL (2) | IL157873A0 (en) |
JO (1) | JO2285B1 (en) |
MA (1) | MA27012A1 (en) |
MX (1) | MXPA03009311A (en) |
MY (1) | MY140271A (en) |
NO (1) | NO20034576L (en) |
NZ (1) | NZ528315A (en) |
PA (1) | PA8543301A1 (en) |
PE (1) | PE20021041A1 (en) |
PL (1) | PL367064A1 (en) |
PT (1) | PT1379511E (en) |
RU (1) | RU2263112C2 (en) |
SI (1) | SI1379511T1 (en) |
SK (1) | SK13682003A3 (en) |
UY (1) | UY27258A1 (en) |
WO (1) | WO2002083652A1 (en) |
YU (1) | YU79003A (en) |
ZA (1) | ZA200307243B (en) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1224175B1 (en) | 1999-10-15 | 2004-03-17 | F. Hoffmann-La Roche Ag | Benzodiazepine derivatives as metabotropic glutamate receptor antagonists |
AU2002359923B2 (en) * | 2001-12-27 | 2007-12-20 | Taisho Pharmaceutical Co., Ltd. | 6-fluorobicyclo[3.1.0]hexane derivatives |
IL163958A0 (en) * | 2002-03-28 | 2005-12-18 | Wisys Technology Foundation | Anxiolytic agents with reduced sedative and ataxideffects |
EP1925614A1 (en) * | 2002-03-28 | 2008-05-28 | Wisys Technology Foundation, Inc. | Anxiolytic agents with reduced sedative and ataxic effects |
RU2357734C2 (en) * | 2003-07-25 | 2009-06-10 | Ф.Хоффманн-Ля Рош Аг | COMBINATION OF mGluR2 RECEPTOR ANTAGONIST AND AChE ENZYME INHIBITOR FOR ACUTE ANDN/OR CHRONIC NEURALGIC DISEASES |
US7329662B2 (en) | 2003-10-03 | 2008-02-12 | Hoffmann-La Roche Inc. | Pyrazolo-pyridine |
US20060160823A1 (en) * | 2004-05-28 | 2006-07-20 | Leonore Witchey-Lakshmanan | Particulate-stabilized injectable pharmaceutical compositions of Posaconazole |
AU2006212457B2 (en) | 2005-02-11 | 2011-04-14 | F. Hoffmann-La Roche Ag | Pyrazolo-pyrimidine derivatives as mGLuR2 antagonists |
CA2602444C (en) | 2005-03-23 | 2013-03-19 | F.Hoffmann-La Roche Ag | Acetylenyl-pyrazolo-pyrimidine derivatives as mglur2 antagonists |
CA2612419C (en) * | 2005-06-23 | 2017-06-13 | Array Biopharma Inc. | Process for preparing benzimidazole compounds |
BRPI0616571A2 (en) | 2005-09-27 | 2011-06-21 | Hoffmann La Roche | oxadiazolyl pyrazol pyridimines as mglur2 antagonists, process for their preparation, pharmaceutical composition containing them and use thereof |
GB0600228D0 (en) * | 2006-01-06 | 2006-02-15 | Fermentas Uab | Inactivation method |
AR059898A1 (en) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | DERIVATIVES OF 3-CIANO-PIRIDONA 1,4-DISUSTITUTED AND ITS USE AS ALLOSTERIC MODULATORS OF MGLUR2 RECEIVERS |
TW200808751A (en) * | 2006-04-13 | 2008-02-16 | Astrazeneca Ab | New compounds |
BRPI0717587A2 (en) | 2006-09-20 | 2013-10-29 | Hoffmann La Roche | 4-OXO-2,3,4,5-TETRA-HYDRO-BENZO DERIVATIVES [B] [1,4] DIAZEPINE |
TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
CN101657432B (en) | 2007-04-19 | 2013-04-10 | 弗·哈夫曼-拉罗切有限公司 | Dihydro-benzo[B][1,4]diazepin-2-one sulfonamide derivatives |
CA2698929C (en) * | 2007-09-14 | 2016-01-19 | Addex Pharma S.A. | 1,3-disubstituted-4-phenyl-1h-pyridin-2-ones |
CN101848893B (en) | 2007-09-14 | 2012-06-06 | 奥梅-杨森制药有限公司 | 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones |
MY152078A (en) | 2007-09-14 | 2014-08-15 | Ortho Mcneil Janssen Pharm | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
MX2010005110A (en) | 2007-11-14 | 2010-09-09 | Ortho Mcneil Janssen Pharm | Imidazo[1,2-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors. |
JP5547194B2 (en) | 2008-09-02 | 2014-07-09 | ジャンセン ファーマシューティカルズ, インコーポレイテッド. | 3-Azabicyclo [3.1.0] hexyl derivatives as modulators of metabotropic glutamate receptors |
EP2346505B1 (en) | 2008-10-16 | 2014-04-23 | Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
CN102232074B (en) | 2008-11-28 | 2014-12-03 | 奥梅-杨森制药有限公司 | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
MX2011011964A (en) | 2009-05-12 | 2012-02-23 | Janssen Pharmaceuticals Inc | 1,2,4-triazolo [4,3-a] pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders. |
AU2010246607B2 (en) | 2009-05-12 | 2012-09-27 | Addex Pharma S.A. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
EP2593447B1 (en) | 2010-07-15 | 2016-08-17 | Bayer Intellectual Property GmbH | 3-pyridyl-heteroarylcarboxamide compounds as pesticides |
WO2012059431A1 (en) | 2010-11-01 | 2012-05-10 | Abbott Gmbh & Co. Kg | Benzenesulfonyl or sulfonamide compounds suitable for treating disorders that respond to the modulation of the serotonin 5-ht6 receptor |
WO2012059432A1 (en) | 2010-11-01 | 2012-05-10 | Abbott Gmbh & Co. Kg | N-phenyl-(homo)piperazinyl-benzenesulfonyl or benzenesulfonamide compounds suitable for treating disorders that respond to the modulation of the 5-ht6 receptor |
PL2649069T3 (en) | 2010-11-08 | 2016-01-29 | Janssen Pharmaceuticals Inc | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
WO2012062759A1 (en) | 2010-11-08 | 2012-05-18 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
CN103261195B (en) | 2010-11-08 | 2015-09-02 | 杨森制药公司 | The purposes of 1,2,4-triazolo [4,3-a] pyridine derivate and the positive allosteric modulators as MGLUR2 acceptor thereof |
JP6240063B2 (en) * | 2011-04-28 | 2017-11-29 | ザ ブロード インスティテュート, インコーポレイテッド | Histone deacetylase inhibitor |
JP5790195B2 (en) * | 2011-06-22 | 2015-10-07 | セントラル硝子株式会社 | Method for producing pyrazole compound |
CA2847247C (en) | 2011-08-29 | 2019-10-15 | Sanford-Burnham Medical Research Institute | Benzodiazepinones as modulators of metabotropic glutamate receptor functions and neurological uses thereof |
JP6337255B2 (en) | 2012-07-27 | 2018-06-06 | ザ ブロード インスティテュート, インコーポレーテッドThe Broad Institute, Inc. | Inhibitors of histone deacetylase |
RU2015116749A (en) | 2012-10-23 | 2016-12-20 | Ф. Хоффманн-Ля Рош Аг | MGLU2 / 3 antagonists for the treatment of autistic disorders |
WO2014100438A1 (en) | 2012-12-20 | 2014-06-26 | The Broad Institute, Inc. | Cycloalkenyl hydroxamic acid derivatives and their use as histone deacetylase inhibitors |
BR112015015477B1 (en) | 2012-12-28 | 2022-07-12 | Crystalgenomics, Inc | 2,3-DI-HYDRO-ISOINDOL-1-ONA DERIVATIVES AND METHODS OF USING THEM AS BTK INHIBITORS |
JO3368B1 (en) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
JO3367B1 (en) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE COMPOUNDS AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
HUE045610T2 (en) | 2014-01-21 | 2020-01-28 | Janssen Pharmaceutica Nv | Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use |
EA033889B1 (en) | 2014-01-21 | 2019-12-05 | Янссен Фармацевтика Нв | Combination comprising sv2a ligand and positive allosteric modulator of metabotropic glutamatergic receptor subtype 2 |
CN106257976B (en) | 2014-03-07 | 2021-02-02 | 拜奥克里斯特制药公司 | Human plasma kallikrein inhibitors |
MA39901A (en) | 2014-04-23 | 2017-03-01 | Hoffmann La Roche | Mglu2/3 antagonists for the treatment of intellectual disabilities |
US9969726B2 (en) | 2014-06-10 | 2018-05-15 | Sanford-Burnham Medical Research Institute | Metabotropic glutamate receptor negative allosteric modulators (NAMS) and uses thereof |
CN108727345B (en) * | 2017-04-25 | 2023-06-27 | 广东东阳光药业有限公司 | Preparation method of imidazole ring intermediate |
CN108586447B (en) * | 2018-01-19 | 2021-01-29 | 中国人民解放军第四军医大学 | Benzodiazepine compound and preparation method and application thereof |
SG11202112684SA (en) * | 2019-06-06 | 2021-12-30 | Arcus Biosciences Inc | Processes for preparing aminopyrimidine compounds |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003506440A (en) * | 1999-08-05 | 2003-02-18 | プレサイエント ニューロファーマ インコーポレイテッド | 1,4-Diazepine derivatives for the treatment of diseases associated with the central nervous system |
NZ517999A (en) * | 1999-10-15 | 2004-07-30 | F | Benzodiazepine derivatives |
EP1224175B1 (en) * | 1999-10-15 | 2004-03-17 | F. Hoffmann-La Roche Ag | Benzodiazepine derivatives as metabotropic glutamate receptor antagonists |
-
2002
- 2002-04-02 KR KR1020037013300A patent/KR100566171B1/en not_active IP Right Cessation
- 2002-04-02 SI SI200230163T patent/SI1379511T1/en unknown
- 2002-04-02 EP EP02737911A patent/EP1379511B1/en not_active Expired - Lifetime
- 2002-04-02 WO PCT/EP2002/003644 patent/WO2002083652A1/en active IP Right Grant
- 2002-04-02 DK DK02737911T patent/DK1379511T3/en active
- 2002-04-02 DE DE60205100T patent/DE60205100T2/en not_active Expired - Lifetime
- 2002-04-02 PT PT02737911T patent/PT1379511E/en unknown
- 2002-04-02 NZ NZ528315A patent/NZ528315A/en unknown
- 2002-04-02 CA CA002442557A patent/CA2442557C/en not_active Expired - Fee Related
- 2002-04-02 JP JP2002581408A patent/JP4071115B2/en not_active Expired - Fee Related
- 2002-04-02 BR BR0208891-6A patent/BR0208891A/en not_active Application Discontinuation
- 2002-04-02 MX MXPA03009311A patent/MXPA03009311A/en active IP Right Grant
- 2002-04-02 HU HU0400851A patent/HUP0400851A3/en unknown
- 2002-04-02 AT AT02737911T patent/ATE299868T1/en not_active IP Right Cessation
- 2002-04-02 YU YU79003A patent/YU79003A/en unknown
- 2002-04-02 AU AU2002312788A patent/AU2002312788B2/en not_active Ceased
- 2002-04-02 PL PL02367064A patent/PL367064A1/en not_active Application Discontinuation
- 2002-04-02 CN CNB028081811A patent/CN1264825C/en not_active Expired - Fee Related
- 2002-04-02 CZ CZ20033003A patent/CZ20033003A3/en unknown
- 2002-04-02 IL IL15787302A patent/IL157873A0/en active IP Right Grant
- 2002-04-02 SK SK1368-2003A patent/SK13682003A3/en unknown
- 2002-04-02 ES ES02737911T patent/ES2246012T3/en not_active Expired - Lifetime
- 2002-04-02 RU RU2003130637/04A patent/RU2263112C2/en not_active IP Right Cessation
- 2002-04-03 US US10/115,826 patent/US6544985B2/en not_active Expired - Fee Related
- 2002-04-09 AR ARP020101290A patent/AR035816A1/en not_active Application Discontinuation
- 2002-04-09 PA PA20028543301A patent/PA8543301A1/en unknown
- 2002-04-10 PE PE2002000291A patent/PE20021041A1/en not_active Application Discontinuation
- 2002-04-10 JO JO200232A patent/JO2285B1/en active
- 2002-04-11 MY MYPI20021345A patent/MY140271A/en unknown
- 2002-04-11 GT GT200200073A patent/GT200200073A/en unknown
- 2002-04-11 UY UY27258A patent/UY27258A1/en not_active Application Discontinuation
-
2003
- 2003-09-11 IL IL157873A patent/IL157873A/en not_active IP Right Cessation
- 2003-09-16 ZA ZA200307243A patent/ZA200307243B/en unknown
- 2003-10-01 HR HR20030792A patent/HRP20030792A2/en not_active Application Discontinuation
- 2003-10-08 EC EC2003004797A patent/ECSP034797A/en unknown
- 2003-10-08 MA MA27346A patent/MA27012A1/en unknown
- 2003-10-10 NO NO20034576A patent/NO20034576L/en not_active Application Discontinuation
- 2003-10-10 BG BG108254A patent/BG108254A/en unknown
-
2005
- 2005-02-24 HK HK05101555A patent/HK1068888A1/en not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR0208891A (en) | Dihydro-benzo [b] - [1,4] diazepin-2-one derivatives as mglur2 ii antagonists | |
BR0208887A (en) | Dihydro-benzo derivatives [b] [1,4] diazepin-2-one as mglur2 i antagonists | |
BR0307474A (en) | Dihydrobenzodiazepin-one derivatives ii | |
BR0211863A (en) | 1-alkyl or 1-cycloalkyltriazolo [4,3a] quinazolin-5-ones as phosphodiesterase inhibitors | |
BR0014326A (en) | Compound, medication, use of compounds, and process for preparing compounds | |
BR0210537A (en) | Crystalline anticholinergic, process for its preparation and its application for the preparation of a medicine | |
BRPI0410029B8 (en) | substituted dihydroquinazoline compound, process for its preparation, medicine comprising said compound and use of said compound | |
BR9911482A (en) | Compound, pharmaceutical composition, use of the compound, and, processes for the treatment or prophylaxis of inflammatory diseases, and for the preparation of a compound | |
BRPI0512335A (en) | compounds, process for their manufacture, pharmaceutical compositions comprising them, method for treating and / or preventing diseases and their use | |
BRPI0112986B8 (en) | azabicyclic compounds, process for their preparation, as well as pharmaceutical compositions comprising said compounds | |
BRPI0407387A (en) | Nitrogen-substituted hexahydropyrazine [1,2-a] pyrimidin-4,7-dione derivatives, processes for their preparation and their application with medicament | |
BR0312560A (en) | New tricyclic spiropiperidines or spiropyrrolidines | |
BR0112586A (en) | Tetrahydroheterocycloaze pyrimidine derivatives | |
BRPI0215312B8 (en) | compound, use of a compound, pharmaceutical composition, and process for preparing a compound | |
BR0108678A (en) | New compounds | |
BR0206935A (en) | Compound, pharmaceutical formulation, use of a compound, method of treatment and / or prophylaxis of conditions associated with glycogen synthase kinase-3 inhibition, and process for preparing a compound | |
BR0013316A (en) | Substituted derivatives of 2-dialkylaminoalkylbiphenyl, their manufacturing process and their use. | |
BR0013311A (en) | Substituted 1,5-dihydropyrrol-2-one derivatives effective as nmda receptor antagonists for the treatment of pain states | |
BR9907934A (en) | Compound, pharmaceutical composition, and process for preparing the compound | |
BR9803704A (en) | Quinazoline-4-one as ampa antagonists. | |
BRPI0418255A (en) | unsubstituted piperazine and piperidine derivatives | |
BR0015322A (en) | Derivatives of indene-, naphtha- and benzocyclohepta-dihydrothiazole, their preparation and their use as anoretic drugs | |
BR9909739A (en) | Benzothiadiazoles and derivatives | |
BR9916680A (en) | Derivatives of 3,3-biarylpiperidine and 2,2-biarylmorpholine | |
BR0206549A (en) | Use of flumazenil in the production of a drug for the treatment of alcohol dependence |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B06A | Patent application procedure suspended [chapter 6.1 patent gazette] | ||
B11B | Dismissal acc. art. 36, par 1 of ipl - no reply within 90 days to fullfil the necessary requirements |